Canonical Allele Identifier: CA2082750212

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32326143_32326144delinsTA , CM000675.2:g.32326143_32326144delinsTA	GRCh38
NC_000013.10:g.32900280_32900281delinsTA , CM000675.1:g.32900280_32900281delinsTA	GRCh37
NC_000013.9:g.31798280_31798281delinsTA	NCBI36
NG_012772.3:g.15664_15665delinsTA , LRG_293:g.15664_15665delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.468_469delinsTA	ENSP00000434898.2:p.Asp156=
ENST00000528762.2:c.468_469delinsTA	ENSP00000433168.2:p.Asp156=
ENST00000530893.7:c.99_100delinsTA	ENSP00000499438.2:p.Asp33=
ENST00000665585.2:c.468_469delinsTA	ENSP00000499570.2:p.Asp156=
ENST00000666593.2:c.468_469delinsTA	ENSP00000499256.2:p.Asp156=
ENST00000700202.2:c.468_469delinsTA	ENSP00000514856.2:p.Asp156=
ENST00000700200.1:n.339_340delinsTA
ENST00000700201.1:c.*247_*248delinsTA	ENSP00000514855.1:n.*247_*248delinsTA
ENST00000380152.8:c.468_469delinsTA MANE Select	ENSP00000369497.3:p.Asp156=
ENST00000544455.6:c.468_469delinsTA	ENSP00000439902.1:p.Asp156=
ENST00000614259.2:c.468_469delinsTA	ENSP00000506251.1:p.Asp156=
ENST00000680887.1:c.468_469delinsTA	ENSP00000505508.1:p.Asp156=
ENST00000380152.7:c.468_469delinsTA	ENSP00000369497.3:p.Asp156=
ENST00000530893.6:n.666_667delinsTA
ENST00000544455.5:c.468_469delinsTA	ENSP00000439902.1:p.Asp156=
ENST00000614259.1:n.468_469delinsTA
NM_000059.3:c.468_469delinsTA , LRG_293t1:c.468_469delinsTA	NP_000050.2:p.Asp156=
XM_011535203.1:c.468_469delinsTA	XP_011533505.1:p.Asp156=
XM_011535204.1:c.468_469delinsTA	XP_011533506.1:p.Asp156=
XM_011535205.1:c.468_469delinsTA	XP_011533507.1:p.Asp156=
NM_000059.4:c.468_469delinsTA MANE Select	NP_000050.3:p.Asp156=